Although exempt research is exempt from some of the federal regulations, in most cases of interaction with participants, a consent process is indicated. It’s important to understand that even though ...

Read this article to learn about online informed consent training for clinical trials, using a collaborative approach.

For research involving collection of biological or tissue specimens in conjunction with a clinical protocol: A statement on retention and future use of biological or tissue specimens within the body ...

Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

All protocols must detail the informed consent process personnel will use if participants will be involved in the research study. Protocols must use the W&M-approved Informed Consent Form (ICF) linked ...

Documentation waivers also allow for online surveys to have a consent process on the first page, ending with a statement like "by clicking the ‘next’ button I agree to participate in the research ...

The informed consent requirements introduced via the Revised Common Rule are listed below. These requirements apply to the following types of studies reviewed by the UNR IRB: Greater than minimal risk ...

introducing a bill that would make it illegal in the state to perform medical research on a corpse without explicit consent. The proposal is a direct response to NBC News’ “Dealing the Dead ...

It is the policy of Western Michigan University that all research involving human subjects will be reviewed by the Institutional Review Board. The involvement of human subjects in research is not ...

introducing a bill that would make it illegal in the state to perform medical research on a corpse without explicit consent. The proposal is a direct response to NBC News’ “Dealing the Dead ...